Dermatome HP NDC 44911-0569

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0569Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0569Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0569-1	44911056901	30 mL in 1 BOTTLE, GLASS (44911-0569-1)Marketed from May 19, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Dermatome HP
Generic name (nonproprietary): lycopodicum clavatum, mezereum, natrum muriaticum,
Active ingredients: Lycopodium clavatum spore — 30 [hp_X]/mLDaphne mezereum bark — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLNitric acid — 30 [hp_X]/mLRanunculus bulbosus — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLThuja occidentalis leaf — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 19, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0569_051b7db5-1b70-4c74-b13f-65037700f1ccSPL ID 051b7db5-1b70-4c74-b13f-65037700f1ccSPL set ID 54a096ac-7ebe-4565-b1b0-0473de16e70cUNII C88X29Y479, X2N6E405GV, 451W47IQ8X, 411VRN1TV4, AEQ8NXJ0MB, 6IO182RP7A, QDL83WN8C2, 0T0DQN8786UPC 0363113701104

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911056901 followed by a unit qualifier and the quantity

Package 44911-0569-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Oct 24, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms associated with herpetic eruptions, such as rashes and cold sores.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)